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Dietary selection of metabolically distinct microorganisms drives hydrogen metabolism in ruminants

Ruminants are important for global food security but emit the greenhouse gas methane. Rumen microorganisms break down complex carbohydrates to produce volatile fatty acids and molecular hydrogen. This hydrogen is mainly converted into methane by archaea, but can also be used by hydrogenotrophic acet...

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Autores principales: Li, Qiu Shuang, Wang, Rong, Ma, Zhi Yuan, Zhang, Xiu Min, Jiao, Jin Zhen, Zhang, Zhi Gang, Ungerfeld, Emilio M., Yi, Kang Le, Zhang, Bai Zhong, Long, Liang, Long, Yun, Tao, Ye, Huang, Tao, Greening, Chris, Tan, Zhi Liang, Wang, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9562222/
https://www.ncbi.nlm.nih.gov/pubmed/35931768
http://dx.doi.org/10.1038/s41396-022-01294-9
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author Li, Qiu Shuang
Wang, Rong
Ma, Zhi Yuan
Zhang, Xiu Min
Jiao, Jin Zhen
Zhang, Zhi Gang
Ungerfeld, Emilio M.
Yi, Kang Le
Zhang, Bai Zhong
Long, Liang
Long, Yun
Tao, Ye
Huang, Tao
Greening, Chris
Tan, Zhi Liang
Wang, Min
author_facet Li, Qiu Shuang
Wang, Rong
Ma, Zhi Yuan
Zhang, Xiu Min
Jiao, Jin Zhen
Zhang, Zhi Gang
Ungerfeld, Emilio M.
Yi, Kang Le
Zhang, Bai Zhong
Long, Liang
Long, Yun
Tao, Ye
Huang, Tao
Greening, Chris
Tan, Zhi Liang
Wang, Min
author_sort Li, Qiu Shuang
collection PubMed
description Ruminants are important for global food security but emit the greenhouse gas methane. Rumen microorganisms break down complex carbohydrates to produce volatile fatty acids and molecular hydrogen. This hydrogen is mainly converted into methane by archaea, but can also be used by hydrogenotrophic acetogenic and respiratory bacteria to produce useful metabolites. A better mechanistic understanding is needed on how dietary carbohydrates influence hydrogen metabolism and methanogenesis. We profiled the composition, metabolic pathways, and activities of rumen microbiota in 24 beef cattle adapted to either fiber-rich or starch-rich diets. The fiber-rich diet selected for fibrolytic bacteria and methanogens resulting in increased fiber utilization, while the starch-rich diet selected for amylolytic bacteria and lactate utilizers, allowing the maintenance of a healthy rumen and decreasing methane production (p < 0.05). Furthermore, the fiber-rich diet enriched for hydrogenotrophic methanogens and acetogens leading to increased electron-bifurcating [FeFe]-hydrogenases, methanogenic [NiFe]- and [Fe]-hydrogenases and acetyl-CoA synthase, with lower dissolved hydrogen (42%, p < 0.001). In contrast, the starch-rich diet enriched for respiratory hydrogenotrophs with greater hydrogen-producing group B [FeFe]-hydrogenases and respiratory group 1d [NiFe]-hydrogenases. Parallel in vitro experiments showed that the fiber-rich selected microbiome enhanced acetate and butyrate production while decreasing methane production (p < 0.05), suggesting that the enriched hydrogenotrophic acetogens converted some hydrogen that would otherwise be used by methanogenesis. These insights into hydrogen metabolism and methanogenesis improve understanding of energy harvesting strategies, healthy rumen maintenance, and methane mitigation in ruminants.
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spelling pubmed-95622222022-10-15 Dietary selection of metabolically distinct microorganisms drives hydrogen metabolism in ruminants Li, Qiu Shuang Wang, Rong Ma, Zhi Yuan Zhang, Xiu Min Jiao, Jin Zhen Zhang, Zhi Gang Ungerfeld, Emilio M. Yi, Kang Le Zhang, Bai Zhong Long, Liang Long, Yun Tao, Ye Huang, Tao Greening, Chris Tan, Zhi Liang Wang, Min ISME J Article Ruminants are important for global food security but emit the greenhouse gas methane. Rumen microorganisms break down complex carbohydrates to produce volatile fatty acids and molecular hydrogen. This hydrogen is mainly converted into methane by archaea, but can also be used by hydrogenotrophic acetogenic and respiratory bacteria to produce useful metabolites. A better mechanistic understanding is needed on how dietary carbohydrates influence hydrogen metabolism and methanogenesis. We profiled the composition, metabolic pathways, and activities of rumen microbiota in 24 beef cattle adapted to either fiber-rich or starch-rich diets. The fiber-rich diet selected for fibrolytic bacteria and methanogens resulting in increased fiber utilization, while the starch-rich diet selected for amylolytic bacteria and lactate utilizers, allowing the maintenance of a healthy rumen and decreasing methane production (p < 0.05). Furthermore, the fiber-rich diet enriched for hydrogenotrophic methanogens and acetogens leading to increased electron-bifurcating [FeFe]-hydrogenases, methanogenic [NiFe]- and [Fe]-hydrogenases and acetyl-CoA synthase, with lower dissolved hydrogen (42%, p < 0.001). In contrast, the starch-rich diet enriched for respiratory hydrogenotrophs with greater hydrogen-producing group B [FeFe]-hydrogenases and respiratory group 1d [NiFe]-hydrogenases. Parallel in vitro experiments showed that the fiber-rich selected microbiome enhanced acetate and butyrate production while decreasing methane production (p < 0.05), suggesting that the enriched hydrogenotrophic acetogens converted some hydrogen that would otherwise be used by methanogenesis. These insights into hydrogen metabolism and methanogenesis improve understanding of energy harvesting strategies, healthy rumen maintenance, and methane mitigation in ruminants. Nature Publishing Group UK 2022-08-05 2022-11 /pmc/articles/PMC9562222/ /pubmed/35931768 http://dx.doi.org/10.1038/s41396-022-01294-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Li, Qiu Shuang
Wang, Rong
Ma, Zhi Yuan
Zhang, Xiu Min
Jiao, Jin Zhen
Zhang, Zhi Gang
Ungerfeld, Emilio M.
Yi, Kang Le
Zhang, Bai Zhong
Long, Liang
Long, Yun
Tao, Ye
Huang, Tao
Greening, Chris
Tan, Zhi Liang
Wang, Min
Dietary selection of metabolically distinct microorganisms drives hydrogen metabolism in ruminants
title Dietary selection of metabolically distinct microorganisms drives hydrogen metabolism in ruminants
title_full Dietary selection of metabolically distinct microorganisms drives hydrogen metabolism in ruminants
title_fullStr Dietary selection of metabolically distinct microorganisms drives hydrogen metabolism in ruminants
title_full_unstemmed Dietary selection of metabolically distinct microorganisms drives hydrogen metabolism in ruminants
title_short Dietary selection of metabolically distinct microorganisms drives hydrogen metabolism in ruminants
title_sort dietary selection of metabolically distinct microorganisms drives hydrogen metabolism in ruminants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9562222/
https://www.ncbi.nlm.nih.gov/pubmed/35931768
http://dx.doi.org/10.1038/s41396-022-01294-9
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